CN112708875A - Zinc-calcium series phosphating solution - Google Patents
Zinc-calcium series phosphating solution Download PDFInfo
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- CN112708875A CN112708875A CN202011523218.7A CN202011523218A CN112708875A CN 112708875 A CN112708875 A CN 112708875A CN 202011523218 A CN202011523218 A CN 202011523218A CN 112708875 A CN112708875 A CN 112708875A
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- Prior art keywords
- zinc
- calcium
- phosphating
- water
- phosphating solution
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- IHBCFWWEZXPPLG-UHFFFAOYSA-N [Ca].[Zn] Chemical class [Ca].[Zn] IHBCFWWEZXPPLG-UHFFFAOYSA-N 0.000 title claims abstract description 27
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims abstract description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 25
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 20
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims abstract description 14
- 239000011787 zinc oxide Substances 0.000 claims abstract description 10
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims abstract description 9
- KBJMLQFLOWQJNF-UHFFFAOYSA-N nickel(ii) nitrate Chemical compound [Ni+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O KBJMLQFLOWQJNF-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910017604 nitric acid Inorganic materials 0.000 claims abstract description 9
- 239000008367 deionised water Substances 0.000 claims description 3
- 229910021641 deionized water Inorganic materials 0.000 claims description 3
- 239000008399 tap water Substances 0.000 claims description 3
- 235000020679 tap water Nutrition 0.000 claims description 3
- 238000005260 corrosion Methods 0.000 abstract description 17
- 230000007797 corrosion Effects 0.000 abstract description 17
- 239000000243 solution Substances 0.000 description 19
- 238000005406 washing Methods 0.000 description 7
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 6
- 239000011575 calcium Substances 0.000 description 6
- 229910052791 calcium Inorganic materials 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 229910019142 PO4 Inorganic materials 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 4
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 229910001424 calcium ion Inorganic materials 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 239000012224 working solution Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910000365 copper sulfate Inorganic materials 0.000 description 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 2
- 238000005238 degreasing Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000010622 cold drawing Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 150000002500 ions Chemical group 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 229910021645 metal ion Chemical group 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 235000019837 monoammonium phosphate Nutrition 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- YPJKMVATUPSWOH-UHFFFAOYSA-N nitrooxidanyl Chemical compound [O][N+]([O-])=O YPJKMVATUPSWOH-UHFFFAOYSA-N 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
- C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/07—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
- C23C22/08—Orthophosphates
- C23C22/22—Orthophosphates containing alkaline earth metal cations
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Treatment Of Metals (AREA)
Abstract
The invention relates to a zinc-calcium phosphating solution. The zinc-calcium phosphating solution comprises the following phosphoric acid in percentage by mass: 5.0 to 8.0; nitric acid: 2.0 to 4.0; zinc oxide: 2.0 to 4.0: calcium nitrate: 20.0 to 30.0; nickel nitrate: 0.5 to 1.0; accelerator (b): 0.02 to 0.03; the balance being water. The corrosion resistance of the zinc-calcium series phosphating film is improved.
Description
Technical Field
The invention relates to the field of surface chemical treatment of metal materials, in particular to a high-corrosion-resistance moderate-temperature zinc-calcium phosphating solution.
Background
Calcium is one of the most widely used inorganic salt additives in phosphating treatments to date. The use of calcium as a phosphating additive has been recognized as a corrosion inhibitor due to calcium. The 20 th century, the 50s, appeared in the uk first, but the development was slow, with the 20 th century reaching completion in the 80 s. At the end of the 80 s of the 20 th century, people began to research, and the development rapidly progressed through the 90 s of the 20 th century. Through research, the calcium is added, so that the effects of at least improving the performance of the phosphating solution, refining the crystal grains and the film thickness of a phosphating film, greatly enhancing the corrosion resistance of the phosphating film, reducing residues and the like can be achieved. Calcium is added in zinc series phosphating, and calcium ions participate in film formation, so that the zinc-calcium series phosphating is called as zinc-calcium series phosphating according to a component classification method of a phosphating film.
In view of energy conservation, the phosphating solution should be developed towards normal and low temperatures, but the intermediate-temperature phosphating is widely used in factories due to a series of advantages of good corrosion resistance, good bonding force, heat resistance, short treatment time, high production efficiency and the like of the obtained film.
CN104711555A discloses a zinc-calcium series phosphating agent, which comprises the following raw materials in percentage by mass: 2-4% of phosphoric acid, 18-26% of calcium nitrate, 15-20% of zinc nitrate, 1-1.2% of ammonium dihydrogen phosphate, 1-1.2% of sodium dihydrogen phosphate, 0.1-0.5% of tartaric acid, 0.1-0.5% of sodium pyrophosphate, 0.1-0.5% of comprehensive phosphating auxiliary agent and the balance of water.
CN03374714A discloses a zinc-calcium phosphating solution for cold drawing of metal, which is an aqueous solution composed of the following components in percentage by weight: phosphoric acid 315 KG; zinc oxide 75 KG; 400KG calcium nitrate; 200KG of zinc nitrate; diluted nitric acid 50KG additive 75 KG; 300KG of water.
The technological process of zinc-calcium series phosphorization production line includes degreasing, water washing, acid washing, water washing, surface conditioning, phosphorization, water washing and drying. The zinc-calcium series phosphating products are developed to be mature and stable today, the corrosion resistance of a zinc-calcium series phosphating film is about 1 to 3 minutes in a copper sulfate dropping experiment generally, but the corrosion resistance of the existing zinc-calcium series phosphating products cannot meet the requirements of users for some users with higher requirements on the corrosion resistance.
Disclosure of Invention
The invention aims to solve the problem of improving the corrosion resistance of the zinc-calcium phosphating solution and ensure that a phosphating film can be maintained to be not rusted for more than 5 minutes in a copper sulfate dropping experiment.
According to the invention, the zinc-calcium phosphating solution is provided, and the formula comprises the following components in percentage by mass: phosphoric acid: 5.0 to 8.0; nitric acid: 2.0 to 4.0; zinc oxide: 2.0 to 4.0: calcium nitrate: 20.0 to 30.0; nickel nitrate: 0.5 to 1.0; accelerator (b): 0.02 to 0.03; the balance being water.
By changing the formula of the existing zinc-calcium phosphating solution, the proportion of calcium ions and zinc ions participating in the generation of a phosphating film is adjusted, and the types and the contents of an accelerating agent and a corrosion inhibitor are adjusted, so that the fineness and the corrosion resistance of the phosphating film and the stability of the phosphating solution are greatly improved without changing the existing production process.
Preferably, the concentration of phosphoric acid is 85%.
Preferably, the water is deionized water.
Preferably, the water is tap water.
Detailed Description
The formula of the zinc-calcium phosphating solution comprises the following components: phosphoric acid, nitric acid, zinc oxide, calcium nitrate, nickel nitrate, an accelerant and water.
The zinc-calcium phosphating solution according to the specific embodiment of the invention comprises the following components in percentage by mass: phosphoric acid: 5.0 to 8.0; nitric acid: 2.0 to 4.0; zinc oxide: 2.0 to 4.0: calcium nitrate: 20.0 to 30.0; nickel nitrate: 0.5 to 1.0; accelerator (b): 0.02 to 0.03; the balance being water.
The invention researches and develops the phosphating solution aiming at customers with higher corrosion resistance of the phosphating film, thereby improving the corrosion resistance of the phosphated workpiece by one step, and the phosphating film is more delicate, so that the corrosion resistance and the adhesive force of the paint film are greatly improved after the subsequent processes such as electrophoresis or paint spraying and the like are finished.
Phosphoric acid and metal ions form phosphate which is the main component of the phosphating film, and the content of the phosphate directly influences the quality of the film.
Calcium is one of main elements for forming a phosphating film, and nitrate radical accelerates the phosphating and shortens the phosphating time.
Zinc oxide is reacted with Ca2+、Fe2+、H3PO4The reaction forms a phosphating film.
Ni of nickel nitrate2+Mainly improves the phosphorization speed and corrosion resistance in a phosphorized film, and NO3 -It also plays a promoting role.
The addition of the accelerator can accelerate the chemical reaction speed and shorten the phosphating time.
The concentration of the phosphoric acid is 85%; the water can be deionized water or tap water, so that the water taking is convenient and the cost is lower.
Example 1
The zinc-calcium phosphating solution according to the embodiment 1 of the invention has the following formula in percentage by mass: phosphoric acid: 5.0; nitric acid: 4.0; zinc oxide: 4.0: calcium nitrate: 30.0 of the total weight of the mixture; nickel nitrate: 1.0; accelerator (b): 0.03; the balance being water.
The experiment was continued using the following conditions:
1. process flow
Degreasing, washing with water, pickling, washing with water, phosphating, washing with water, standing for 24h and checking
2. Phosphating process conditions
Temperature: 65 + -0.5 deg.C
Time: 0-10min
The corrosion resistance increases with increasing phosphating time, as a result of the increasing deposition of insoluble phosphates on the iron surface with time. However, the corrosion resistance is not linear with time throughout the phosphating process, and the film thickness increases over too long a phosphating period, which may cause a decrease in the adhesion of the primer. Therefore, in the production process, the time can be controlled according to the requirement to obtain ideal corrosion resistance and a certain film thickness, and good bonding force between the substrate and the coating is ensured.
3. Performance test of phosphating film
The spot experiments were carried out according to GB 6807-2001.
Preparing 500ml of working solution, phosphating 10 batches of test pieces, controlling the phosphating area to be 0.07 square meter within 7min, and controlling the free acidity of the phosphating solution to be 2.70-4.00 points. The final measured average drip time was 350 s.
Example 2
Example 2 compared with example 1, except that the mass percentages of the components are changed, the other contents are completely the same, and for the sake of convenience, the same contents are not repeated herein, and the mass percentages of the components of the zinc-calcium phosphating solution of example 2 are as follows: phosphoric acid: 6.0; nitric acid: 3.0; zinc oxide: 3.0: calcium nitrate: 20.0; nickel nitrate: 0.5; accelerator (b): 0.02; the balance being water.
Preparing 500ml of working solution, phosphating 10 batches of test pieces, controlling the phosphating area to be 0.07 square meter within 7min, and controlling the free acidity of the phosphating solution to be 2.70-4.00 points. The final average drop time was measured to be 400 s.
Example 3
Example 3 compared with examples 1 and 2, except that the mass percentages of the components are changed, the other contents are completely the same, and for the sake of convenience, the same contents are not repeated herein, and the mass percentages of the components of the zinc-calcium phosphating solution of example 3 are as follows: the zinc-calcium phosphating solution according to the embodiment 1 of the invention has the following formula in percentage by mass: phosphoric acid: 5.0; nitric acid: 4.0; zinc oxide: 4.0: calcium nitrate: 25.0; nickel nitrate: 0.7; accelerator (b): 0.025; the balance being water.
Preparing 500ml of working solution, phosphating 10 batches of test pieces, controlling the phosphating area to be 0.07 square meter within 7min, and controlling the free acidity of the phosphating solution to be 2.70-4.00 points. The final average drop time was measured to be 360 s.
It is to be understood that the scope of the invention is defined by the claims and that the above examples are illustrative of the invention only.
Claims (4)
1. The zinc-calcium phosphating solution is characterized by comprising the following components in percentage by mass:
phosphoric acid: 5.0 to 8.0;
nitric acid: 2.0 to 4.0;
zinc oxide: 2.0 to 4.0:
calcium nitrate: 20.0 to 30.0;
nickel nitrate: 0.5 to 1.0;
accelerator (b): 0.02 to 0.03;
the balance being water.
2. The zinc-calcium phosphating solution according to claim 1, wherein the concentration of the phosphoric acid is 85%.
3. The zinc-calcium phosphating solution according to claim 1, wherein the water is deionized water.
4. The zinc-calcium phosphating solution according to claim 1, wherein the water is tap water.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202011523218.7A CN112708875A (en) | 2020-12-21 | 2020-12-21 | Zinc-calcium series phosphating solution |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202011523218.7A CN112708875A (en) | 2020-12-21 | 2020-12-21 | Zinc-calcium series phosphating solution |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN112708875A true CN112708875A (en) | 2021-04-27 |
Family
ID=75544918
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202011523218.7A Pending CN112708875A (en) | 2020-12-21 | 2020-12-21 | Zinc-calcium series phosphating solution |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN112708875A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116145123A (en) * | 2023-01-03 | 2023-05-23 | 华南理工大学 | A method for constructing a superhydrophobic anti-corrosion film layer on the surface of a zinc-based coating |
| CN117012534A (en) * | 2023-07-31 | 2023-11-07 | 广东省科学院新材料研究所 | Method for preparing metal magnetic powder core by adopting zinc-calcium phosphating solution |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4140551A (en) * | 1977-08-19 | 1979-02-20 | Heatbath Corporation | Low temperature microcrystalline zinc phosphate coatings, compositions, and processes for using and preparing the same |
| CN86100516A (en) * | 1986-03-03 | 1986-09-10 | 华东添加剂公司 | Zinc-calcium series phosphatating liquid |
| US5328526A (en) * | 1992-04-03 | 1994-07-12 | Nippon Paint Co., Ltd. | Method for zinc-phosphating metal surface |
| CN101245457A (en) * | 2007-02-13 | 2008-08-20 | 天津市永华科贸发展有限责任公司 | Phosphorization liquid and manufacture method thereof |
| CN103374714A (en) * | 2012-04-13 | 2013-10-30 | 上海顶旭化学品有限公司 | Zinc-calcium series phosphating solution for metal cold-drawing |
| CN104087920A (en) * | 2014-06-30 | 2014-10-08 | 姜洪俊 | Zinc phosphating liquid |
-
2020
- 2020-12-21 CN CN202011523218.7A patent/CN112708875A/en active Pending
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4140551A (en) * | 1977-08-19 | 1979-02-20 | Heatbath Corporation | Low temperature microcrystalline zinc phosphate coatings, compositions, and processes for using and preparing the same |
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| Title |
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| 胡煜艳等: "锌钙系磷化液的研究", 《电镀与环保》 * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116145123A (en) * | 2023-01-03 | 2023-05-23 | 华南理工大学 | A method for constructing a superhydrophobic anti-corrosion film layer on the surface of a zinc-based coating |
| CN117012534A (en) * | 2023-07-31 | 2023-11-07 | 广东省科学院新材料研究所 | Method for preparing metal magnetic powder core by adopting zinc-calcium phosphating solution |
| CN117012534B (en) * | 2023-07-31 | 2024-04-30 | 广东省科学院新材料研究所 | A method for preparing metal magnetic powder core using zinc-calcium phosphating solution |
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Application publication date: 20210427 |